ISO 20696:2018
Current
The latest, up-to-date edition.
Sterile urethral catheters for single use
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English, French
05-06-2018
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This document specifies requirements and test methods for sterile urethral catheters for single use, with or without a balloon.
This document does not include drainage catheters covered by ISO 20697, e.g. ureteral catheters, nephrostomy catheters, and suprapubic catheters. This document also excludes ureteral stents.
NOTE Ureteral stents are covered in ASTM F1828‑97.
| Committee |
ISO/TC 84
|
| DevelopmentNote |
Supersedes ISO/DIS 20696. (06/2018)
|
| DocumentType |
Standard
|
| Pages |
0
|
| ProductNote |
THIS STANDARD HAVE CORRECTED VERSION FOR ENGLISH AND FRENCH 2018
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Standards | Relationship |
| DS EN ISO 20696 : 2018 | Identical |
| IS 18288 : 2023 | Identical |
| SN EN ISO 20696:2019 | Identical |
| UNE-EN ISO 20696:2019 | Identical |
| DIN EN ISO 20696:2019-04 | Identical |
| EN ISO 20696:2018 | Identical |
| PN-EN ISO 20696:2018 | Identical |
| NF EN ISO 20696 : 2018 | Identical |
| ÖNORM EN ISO 20696 : 2019 02 01 | Identical |
| UNI EN ISO 20696:2018 | Identical |
| SS-EN ISO 20696:2018 | Identical |
| DIN EN ISO 20696:2020-10 | Identical |
| DIN EN ISO 20696:2018-10 | Identical |
| NEN-EN-ISO 20696:2018 (Cor. 2020-03) | Identical |
| ÖNORM EN ISO 20696:2020 10 15 | Identical |
| I.S. EN ISO 20696:2018 | Identical |
| I.S. EN ISO 20696:2018&LC:2018 | Identical |
| BS EN ISO 20696:2018 | Identical |
| DIN 13273-7:2003-08 | CATHETER FOR MEDICAL USE - PART 7: DETERMINATION OF THE X-RAY ATTENUATION OF CATHETERS - REQUIREMENTS AND TESTING |
| ISO 11135:2014 | Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices |
| ASTM F 1842 : 2015 : REDLINE | Standard Test Method for Determining Ink or Coating Adhesion on Flexible Substrates for a Membrane Switch or Printed Electronic Device |
| ISO/TR 19244:2014 | Guidance on transition periods for standards developed by ISO/TC 84 — Devices for administration of medicinal products and catheters |
| EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
| ASTM F 2052 : 2015 : REDLINE | Standard Test Method for Measurement of Magnetically Induced Displacement Force on Medical Devices in the Magnetic Resonance Environment |
| ASTM F 2213 : 2017 : REDLINE | Standard Test Method for Measurement of Magnetically Induced Torque on Medical Devices in the Magnetic Resonance Environment |
| ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
| ISO 80369-1:2010 | Small-bore connectors for liquids and gases in healthcare applications Part 1: General requirements |
| ASTM F 1828 : 2017 : REDLINE | Standard Specification for Ureteral Stents |
| ISO 14971:2007 | Medical devices Application of risk management to medical devices |
| ISO 15223-1:2016 | Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements |
| EN 980:2008 | Symbols for use in the labelling of medical devices |
| ASTM F 640 : 2012 : REDLINE | Standard Test Methods for Determining Radiopacity for Medical Use |
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